Issue 3, 2016

Stereoselective organocatalysed reactions in deep eutectic solvents: highly tunable and biorenewable reaction media for sustainable organic synthesis

Abstract

Three distinct stereoselective reactions, catalysed by using a chiral primary amine through different activation methods, have been successfully carried out for the first time in bio-based eutectic mixtures, thereby affording functionalised molecules in very high enantioselectivity. The use of these unconventional and biorenewable reaction media also provides opportunities for facilitating the recovery and the recycling of the chiral catalyst.

Graphical abstract: Stereoselective organocatalysed reactions in deep eutectic solvents: highly tunable and biorenewable reaction media for sustainable organic synthesis

Supplementary files

Article information

Article type
Paper
Submitted
10 Aug 2015
Accepted
01 Sep 2015
First published
01 Sep 2015

Green Chem., 2016,18, 792-797

Stereoselective organocatalysed reactions in deep eutectic solvents: highly tunable and biorenewable reaction media for sustainable organic synthesis

E. Massolo, S. Palmieri, M. Benaglia, V. Capriati and F. M. Perna, Green Chem., 2016, 18, 792 DOI: 10.1039/C5GC01855B

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